首页> 外文OA文献 >A Segment of the Apospory-Specific Genomic Region Is Highly Microsyntenic Not Only between the Apomicts Pennisetum squamulatum and Buffelgrass, But Also with a Rice Chromosome 11 Centromeric-Proximal Genomic Region1[W]
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A Segment of the Apospory-Specific Genomic Region Is Highly Microsyntenic Not Only between the Apomicts Pennisetum squamulatum and Buffelgrass, But Also with a Rice Chromosome 11 Centromeric-Proximal Genomic Region1[W]

机译:附子特异的基因组区域的一部分不仅在无融合生殖的象草狼尾草和水牛草之间而且在水稻染色体11着丝粒附近的基因组区域1中都具有高微同调[W]。

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摘要

Bacterial artificial chromosome (BAC) clones from apomicts Pennisetum squamulatum and buffelgrass (Cenchrus ciliaris), isolated with the apospory-specific genomic region (ASGR) marker ugt197, were assembled into contigs that were extended by chromosome walking. Gene-like sequences from contigs were identified by shotgun sequencing and BLAST searches, and used to isolate orthologous rice contigs. Additional gene-like sequences in the apomicts' contigs were identified by bioinformatics using fully sequenced BACs from orthologous rice contigs as templates, as well as by interspecies, whole-contig cross-hybridizations. Hierarchical contig orthology was rapidly assessed by constructing detailed long-range contig molecular maps showing the distribution of gene-like sequences and markers, and searching for microsyntenic patterns of sequence identity and spatial distribution within and across species contigs. We found microsynteny between P. squamulatum and buffelgrass contigs. Importantly, this approach also enabled us to isolate from within the rice (Oryza sativa) genome contig Rice A, which shows the highest microsynteny and is most orthologous to the ugt197-containing C1C buffelgrass contig. Contig Rice A belongs to the rice genome database contig 77 (according to the current September 12, 2003, rice fingerprint contig build) that maps proximal to the chromosome 11 centromere, a feature that interestingly correlates with the mapping of ASGR-linked BACs proximal to the centromere or centromere-like sequences. Thus, relatedness between these two orthologous contigs is supported both by their molecular microstructure and by their centromeric-proximal location. Our discoveries promote the use of a microsynteny-based positional-cloning approach using the rice genome as a template to aid in constructing the ASGR toward the isolation of genes underlying apospory.
机译:用无孢子特异性基因组区域(ASGR)标记ugt197分离的,来自无尾小象盘尾草和水牛(Cenchrus ciliaris)的细菌人工染色体(BAC)克隆组装成重叠群,通过染色体行走延伸。通过散弹枪测序和BLAST搜索鉴定了来自重叠群的基因样序列,并将其用于分离直系同源水稻重叠群。通过生物信息学,使用直系同源水稻重叠群的全序列BAC作为模板,以及通过种间,全重叠群交叉杂交,鉴定了无融合生殖重叠群中的其他基因样序列。通过构建详细的远距离重叠群分子图来显示类基因序列和标记的分布,并搜索物种重叠群内和跨物种重叠群的序列同一性和空间分布的微同构模式,从而快速评估了重叠重叠群的正统学。我们发现鳞茎假单胞菌和水牛草重叠群之间有微同调。重要的是,这种方法还使我们能够从水稻(Oryza sativa)重叠群A中分离出水稻A,该序列显示出最高的微同调性,并且与含ugt197的C1C水牛草重叠群最直系同源。重叠群水稻A属于水稻基因组数据库重叠群77(根据当前的2003年9月12日,水稻指纹重叠群构建),其定位于第11号染色体着丝粒的近端,这一特征与ASGR连锁的BAC的近端的映射有趣地相关。着丝粒或着丝粒样序列。因此,这两个直系同源重叠群之间的相关性由它们的分子微结构和着丝粒近端的位置所支持。我们的发现促进了以水稻基因组为模板的基于微同位的位置克隆方法的使用,以协助构建ASGR来分离无孢子的基因。

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